Canonical Allele Identifier: CA1950237662
Gene: TPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6616968G= , CM000673.2:g.6616968G= GRCh38
NC_000011.9:g.6638199G= , CM000673.1:g.6638199G= GRCh37
NC_000011.8:g.6594775G= NCBI36
NG_008653.1:g.7494C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682424.1:c.573+7C= ENSP00000507321.1:n.573+7C=
ENST00000299427.12:c.687+7C= MANE Select ENSP00000299427.6:n.687+7C=
ENST00000436873.7:c.312+333C=
ENST00000524788.2:n.1846+7C=
ENST00000524903.2:n.1962+7C=
ENST00000528807.2:n.343+7C=
ENST00000530040.2:n.479+391C=
ENST00000533371.6:c.-43+7C= ENSP00000437066.1:n.-43+7C=
ENST00000642892.1:c.-43+7C= ENSP00000494165.1:n.-43+7C=
ENST00000643439.1:c.*427+7C= ENSP00000495849.1:n.*427+7C=
ENST00000643479.1:n.716+7C=
ENST00000643516.1:c.395+333C=
ENST00000644151.1:n.2126+7C=
ENST00000644218.1:c.687+7C= ENSP00000493574.1:n.687+7C=
ENST00000644683.1:c.*140+7C= ENSP00000494085.1:n.*140+7C=
ENST00000644810.1:c.408+7C= ENSP00000495895.1:n.408+7C=
ENST00000644831.1:n.863+7C=
ENST00000644933.1:c.-43+7C= ENSP00000496133.1:n.-43+7C=
ENST00000645020.1:n.1869C=
ENST00000645285.1:c.-43+7C= ENSP00000495058.1:n.-43+7C=
ENST00000645331.1:n.1053+7C=
ENST00000645620.1:c.-43+7C= ENSP00000493657.1:n.-43+7C=
ENST00000646777.1:n.863+7C=
ENST00000647016.1:n.1167+7C=
ENST00000647152.1:c.-43+7C= ENSP00000495893.1:n.-43+7C=
ENST00000647209.1:c.*556+7C= ENSP00000495558.1:n.*556+7C=
ENST00000647346.1:n.1707+7C=
ENST00000299427.10:c.687+7C= ENSP00000299427.6:n.687+7C=
ENST00000436873.6:c.450+391C= ENSP00000398136.2:n.450+391C=
ENST00000524788.1:n.387+7C=
ENST00000528807.1:n.237+7C=
ENST00000533371.5:c.-43+7C= ENSP00000437066.1:n.-43+7C=
ENST00000611494.4:c.687+7C= ENSP00000484546.1:n.687+7C=
NM_000391.3:c.687+7C= NP_000382.3:n.687+7C=
NM_000391.4:c.687+7C= MANE Select NP_000382.3:n.687+7C=